neurodevelopmental disorder with hypotonia and characteristic brain abnormalities
MONDO:0958278Mondo
Findings
No curated finding names neurodevelopmental disorder with hypotonia and characteristic brain abnormalities yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset · Neonatal onset
HPO, annotations 2026-09-02
Features
51 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- AtaxiaHPOHP:0001251
- 2 of 2 reported patients
- HypotoniaHPOHP:0001252
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 15 of 16 reported patients
- Axial hypotoniaHPOHP:0008936
- 13 of 15 reported patients
- Slit-like lateral ventricleHPOHP:6000989
- 3 of 5 reported patients
- Absent speechHPOHP:0001344
- 6 of 11 reported patients
- Gray matter heterotopiaHPOHP:0002282
- 3 of 7 reported patients
- Short corpus callosumHPOHP:0200012
- 3 of 7 reported patients
- Thin corpus callosumHPOHP:0033725
- 3 of 7 reported patients
- Aggressive behaviorHPOHP:0000718
- 2 of 5 reported patients
- Ankle contractureHPOHP:0034677
- 2 of 5 reported patients
- Appendicular hypotoniaHPOHP:0012389
- 6 of 15 reported patients
Show the remaining 39
- Appendicular spasticityHPOHP:0034353
- 2 of 5 reported patients
- Failure to thriveHPOHP:0001508
- 4 of 10 reported patients
- HyperreflexiaHPOHP:0001347
- 2 of 5 reported patients
- HypotelorismHPOHP:0000601
- 2 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 6 of 15 reported patients
- Posteriorly rotated earsHPOHP:0000358
- 2 of 5 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- SLC4A10HGNC:13811
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · Baylor College of Medicine Research Center · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2025